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EP1046682B1 - Revêtements aqueux pigmentés - Google Patents

Revêtements aqueux pigmentés Download PDF

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Publication number
EP1046682B1
EP1046682B1 EP00108646A EP00108646A EP1046682B1 EP 1046682 B1 EP1046682 B1 EP 1046682B1 EP 00108646 A EP00108646 A EP 00108646A EP 00108646 A EP00108646 A EP 00108646A EP 1046682 B1 EP1046682 B1 EP 1046682B1
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Prior art keywords
weight
polymer
monomers
coating composition
composition according
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EP00108646A
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German (de)
English (en)
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EP1046682A1 (fr
Inventor
Cheng-Le Zhao
Uwe Dittrich
Manfred Schwartz
Gernot Franzmann
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BASF SE
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BASF SE
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04—Homopolymers or copolymers of esters
    • C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/062—Copolymers with monomers not covered by C09D133/06
    • C09D133/064—Copolymers with monomers not covered by C09D133/06 containing anhydride, COOH or COOM groups, with M being metal or onium-cation
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/46—Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with organic materials
    • C04B41/48—Macromolecular compounds
    • C04B41/483—Polyacrylates
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/60—After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone of only artificial stone
    • C04B41/61—Coating or impregnation
    • C04B41/62—Coating or impregnation with organic materials
    • C04B41/63—Macromolecular compounds

Definitions

  • the present invention relates to aqueous, substantially solvent-free, Pigment-containing coating compositions containing at least a dispersion of a film-forming polymer P included.
  • Pigment-containing, aqueous coating compositions contained as a binder for the pigment particles and optionally present Fillers usually a film-forming polymer in the form of a aqueous polymer dispersion.
  • the contained in the polymer dispersion Polymer particles form during drying of the coating Polymer film that binds the pigment particles and the fillers.
  • MFT temperature above the polymer in the coating agent forms a polymer film
  • a low minimum film-forming temperature can basically by using a polymeric binder be achieved with a low glass transition temperature.
  • polymers Binder with a low glass transition temperature However, they have the disadvantage that the polymer film is soft and sticky is.
  • Coating agents therefore usually contain a polymer having a higher glass transition temperature and a film-forming assistant, which lowers the film-forming temperature of the polymer.
  • the film-forming aids acts they are usually volatile organic compounds, for example to solvents or plasticizers when drying the coating initially facilitate film formation. At the next The film-forming aids are dried to the environment which increases the surface hardness of the polymer film and his stickiness humiliated. The delivery of such However, volatile substances to the environment provides a strong It is therefore desirable to use film-forming aids and other volatile components in pigmented, to avoid aqueous coating agents.
  • binders for Solvent-free, aqueous coating compositions which special esters of acrylic acid or methacrylic acid with polyethylene glycols (PEG monomers) in copolymerized form.
  • PEG-monomers are comparatively expensive and not effective in their effect always satisfactory.
  • EP-A-327 006 describes aqueous polymer dispersions which contained in small amounts silane monomers in copolymerized form. Such Polymer dispersions are also used as binders for low-solvent Coating suitable. Already a small one However, incorporation of silane monomers increases manufacturing costs for the binder polymers to a considerable extent.
  • binder polymers for solvent-free Emulsion paints known as binder polymers Step polymers of a hard and a soft Contain polymers.
  • the present invention is therefore based on the object to provide aqueous, pigment-containing coating compositions which to coatings with good wet abrasion resistance and low soiling tendency lead and which are essentially free of organic Volatile compounds such as plasticizers and solvents.
  • the binder polymer without expensive production process or the use of costly specialty monomers be produced.
  • the coatings should also in particular against exposure to UV radiation, i. during prolonged weathering be stable.
  • pigment-containing coating compositions that are essentially free of volatile, organic compounds and their binder polymer substantially composed of esters of acrylic acid and / or methacrylic acid is, to coatings with a low soiling tendency and good weathering stability when the coating agent a small amount, but less than 0.3 wt .-%, based on the polymer, a non-polymerizable photoinitiator contains.
  • the coating compositions according to the invention generally contain less than 0.5%, preferably less than 0.1%, especially less than 500 ppm and especially less than 300 ppm volatile organic Links. These include organic solvents, Plasticizer (organic liquids with a boiling point above 250 ° C) and - production-related - unpolymerized monomers (so-called residual monomers).
  • the coating compositions of the invention contained as volatile, organic compounds preferably no additives such as solvents or plasticizers, but exclusively production-related, volatile organic Impurities such as residual monomers and their conversion products.
  • the content of residual monomers in the coating compositions of the invention is advantageously below 300 ppm and in particular below 200 ppm.
  • the pigment volume concentration PVK is by definition the one with 100 multiplied quotient of the total volume of the coating agent divided fillers and pigments by the total volume of fillers, pigments and binder polymer, here polymer P.
  • the minimum film-forming temperature (MFT) of the dispersion of the polymer P is below its processing temperature.
  • the difference between processing temperature and minimum film-forming temperature is at least 5 K and especially at least 10 K.
  • the minimum film-forming temperature of the aqueous dispersion of the polymer P will be below 10 ° C and especially below 5 ° C.
  • the minimum film forming temperatures are the values determined on the basis of DIN 53787 (see Ullmann's Enzyklopadie der Technischen Chemie, 4th edition Bd.19, VCH Weinheim 1980, p. 17).
  • the adjustment of the MFT by selecting a polymer P with a suitable glass transition temperature T G is generally up to 15 K below its glass transition temperature T G.
  • the glass transition temperature of the polymer P is preferably chosen below 25 ° C. and in particular below 15 ° C. If elevated processing temperatures are possible, for example in regions with elevated ambient temperature, the polymer P may of course also have a higher glass transition temperature, for example up to 30 ° C.
  • the glass transition temperature T G does not fall below a value of -25 ° C and especially -10 ° C in order to ensure a sufficient hardness and strength of the polymer film.
  • glass transition temperature means in this document according to the DSC method (differential scanning calorimetry, 20 ° C / min, midpoint) determined glass transition temperature (see. ASTM D 3418-82).
  • the non-polymerizable photoinitiators according to the invention are generally compounds which cause a crosslinking reaction of the polymers P by the action of sunlight.
  • compounds having a diaryl ketone structure such as benzophenone, thioxanthone and their derivatives are suitable.
  • one or both phenyl rings are mono- or polysubstituted.
  • Suitable substituents are C 1 -C 4 -alkyl, for example methyl, hydroxy, C 1 -C 4 -alkyloxy, hydroxy-C 1 -C 4 -alkyl, hydroxy-C 1 -C 4 -alkyloxy, amino, C 1 -C 4- alkylamino, nitro, carboxyl, carboxy-C 1 -C 4 -alkyl, for example carboxymethyl, acyloxy such as acryloxy and methacryloxy and nitro. Also suitable are substituents which give the photoinitiator increased water solubility.
  • Such substituents have neutral or ionic groups such as trialkylammonium, eg triethylammonium, trimethylammonium, sulfonate, carboxylate or polyalkylene oxide.
  • substituents are: trimethylammoniummethyl, trimethylammoniumpropyloxy, 2-hydroxy-3-trimethylammonium (each as chloride), sulfomethyl, 3-sulfopropyloxy (each as sodium salt) and HO (C 2 H 4 -O) n -, with n of 2 to 100.
  • Preferred according to the invention are benzophenone and its derivatives.
  • benzophenone derivatives in which only one of the phenyl rings carries substituents, especially those having only one substituent and especially those wherein this substituent is in the 4-position of the phenyl ring.
  • substituents especially those having only one substituent and especially those wherein this substituent is in the 4-position of the phenyl ring.
  • particularly suitable derivatives of benzophenone are 4-methylbenzophenone, 4-hydroxybenzophenone, 4-aminobenzophenone, 4-chlorobenzophenone, 4-carboxybenzophenone, 4,4'-dimethylbenzophenone, 4,4'-dichlorobenzophenone, 4-carboxymethylbenzophenone, 3-nitrobenzophenone and 2,4,6-trimethyl.
  • Benzophenone is particularly preferably used as inventive non-polymerizable photoinitiator, wherein mixtures of benzophenone and suitable auxiliary substances which are liquid at room temperature are likewise advantageous in terms of their application.
  • the photoinitiators are used in an amount of less than 0.3% by weight, based on the polymer P, in the coating agent.
  • the amount of photoinitiator used is preferably above 0.05% by weight and in particular above 0.1% by weight. Preferably, it is up to 0.25 wt .-%, based on the polymer P. In particular, use amounts of about 0.1 to 0.25 wt.%, Based on polymer P, benzophenone, optionally as a mixture with 1-hydroxy -1-benzoylcyclohexane proven.
  • the polymer P used according to the invention as a binder is essentially, ie at least 80% by weight, based on the total weight of the polymer P, of esters of acrylic acid and / or esters of methacrylic acid with C 1 -C 20 -, preferably C 1 - C 12 - and in particular C 1 -C 8 -alkanols or C 5 -C 10 -cycloalkanols (monomers A).
  • C 1 -C 20 -alkanols examples include methanol, ethanol, n-propanol, isopropanol, 1-butanol, 2-butanol, isobutanol, tert-butanol, n-hexanol, 2-ethylhexanol, lauryl alcohol and stearyl alcohol .
  • Suitable cycloalkanols are, for example, cyclopentanol, cyclohexanol, 4-tert-butylcyclohexan-1-ol, 3,3,5-trimethylcyclohexan-1-ol and isoborneol.
  • Preferred monomers A are C 1 -C 4 -alkyl methacrylates such as methyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, and tert-butyl methacrylate, furthermore C 2 -C 10 -alkyl acrylates such as ethyl acrylate, n-butyl acrylate, tert-butyl acrylate, n-hexyl acrylate, n Octyl acrylate, 2-ethylhexyl acrylate, decyl acrylate and 2-propylheptyl acrylate.
  • C 1 -C 4 -alkyl methacrylates such as methyl methacrylate, n-butyl methacrylate, isobutyl methacrylate, and tert-butyl methacrylate
  • C 2 -C 10 -alkyl acrylates such as ethyl acrylate, n-
  • the polymers P used in the coating compositions according to the invention also contain, based on their total weight, 0.05 to 10% by weight, preferably 0.1 to 5% by weight and in particular 0.2 to 3% by weight, of at least one Monomers B selected from ethylenically unsaturated carboxylic acids, ethylenically unsaturated sulfonic acids, ethylenically unsaturated phosphonic acids and their salts, in particular their sodium, potassium and ammonium salts.
  • Monomers B selected from ethylenically unsaturated carboxylic acids, ethylenically unsaturated sulfonic acids, ethylenically unsaturated phosphonic acids and their salts, in particular their sodium, potassium and ammonium salts.
  • ethylenically unsaturated carboxylic acids are monoethylenically unsaturated C 3 -C 8 -monocarboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, vinylacetic acid, acrylamidoglycolic acid and methacrylamidoglycolic acid, furthermore monoethylenically unsaturated C 4 -C 8 -dicarboxylic acids such as maleic acid, fumaric acid, itaconic acid, and citraconic acid, furthermore their Half esters with C 1 -C 10 -alkanols, such as monomethylmaleinate and mono-n-butylmaleinate.
  • C 3 -C 8 -monocarboxylic acids such as acrylic acid, methacrylic acid, crotonic acid, vinylacetic acid, acrylamidoglycolic acid and methacrylamidoglycolic acid, furthermore monoethylenically unsaturated C 4 -C 8 -dicarboxylic acids such as
  • Examples of ethylenically unsaturated sulfonic acids are vinylsulfonic acid, 2-acrylamido-2-methylpropanesulfonic acid, 2-acryloxyethanesulfonic acid, 3-acryloxypropanesulfonic acid, vinylbenzenesulfonic acid.
  • Examples of suitable phosphonic acids are vinylphosphonic acid, allylphosphonic acid and 2-acrylamido-2-methylpropanephosphonic acid.
  • Preferred monomers B are acrylic acid, methacrylic acid and itaconic acid. For coating compositions with high wet abrasion resistance, it has proven useful if the monomers B, based on the total weight of the monomers B, comprise at least 50% itaconic acid.
  • the invention applied polymers P up to 20 wt .-%, based on the total weight of the polymer P, monomers C, of the The above monomers A and B are different.
  • the monomers C include, on the one hand, monomers which are active in the radical Emulsion polymerization also to Polymerlatices polymerize. These include in particular vinyl esters aliphatic Carboxylic acids such as vinyl acetate, vinyl propionate and Vinylversatate and vinyl aromatic compounds such as styrene.
  • Preferred monomers C are neutral monomers having an increased water solubility, ie> 100 g / l (at 25 ° C), which are preferably used in amounts of up to 10 wt .-%, for example 0.1 to 5 wt .-%.
  • amides of the abovementioned monoethylenically unsaturated C 3 -C 8 -monocarboxylic acids such as acrylamide and methacrylamide, furthermore their hydroxyalkyl esters such as hydroxyethyl acrylate, hydroxypropyl acrylate, 4-hydroxybutyl acrylate and the corresponding methacrylates, furthermore water-soluble N-vinyllactams, for example N-vinylpyrrolidone.
  • Particularly preferred monomers C are acrylamide and methacrylamide.
  • the monomers C further include such monomers, the urea groups have, e.g. N-vinyl and N-allyl urea and Derivatives of imidazolidin-2-one, e.g. N-vinyl and N-allylimidazolidin-2-one, N-vinyloxyethylimidazolidin-2-one, N- (2- (meth) acrylamidoethyl) imidazolidin-2-one, N- (2- (meth) acryloxyethyl) imidazolidin-2-one, N- [2 - ((meth) acryloxyacetamido) -ethyl] imidazolidin-2-one etc.
  • the urea groups have, e.g. N-vinyl and N-allyl urea and Derivatives of imidazolidin-2-one, e.g. N-vinyl and N-allylimidazolidin-2-one, N-vinyloxy
  • These monomers are preferably used in amounts of up to 10 wt .-%, in particular 0.5 to 5 wt .-%, based on the total weight of the polymer P. Improve such monomers the wet adhesion of the available from the preparations of the invention Coatings, i. the adhesion of the coating in damp or swollen condition.
  • the monomers C furthermore include siloxane groups
  • Monomers e.g. Vinyltrialkoxysilanes, such as vinyltrimethoxysilane, Alkylvinyldialkoxysilanes or (meth) acryloxyalkyltrialkoxysilanes, e.g. (Meth) acryloxyethyltrimethoxysilane, (meth) acryloxypropyltrimethoxysilane.
  • These monomers can be used in amounts of up to 1 wt .-%, preferably 0.05 to 0.5 wt .-%, based on the total amount of monomers, be used.
  • the polymer particles in the binder polymer dispersion a weight average Polymer particle diameter in the range of 50 to 1000 nm (determined by ultracentrifuge or photon correlation spectroscopy; for particle size determination by means of ultracentrifuge see, e.g. W. Gurchtle, Macromolecular Chemistry, 1984, Vol. 185, 1025-1039, W. Gurchtle, Angew. Macromolecular Chemistry, 1988, 162, 35-42).
  • For binder dispersions with high solids levels e.g.
  • the weight average particle diameter the polymer particle in the dispersion is ⁇ 100 nm.
  • the average particle diameter will preferably not exceed 600 nm.
  • the preparation of the aqueous dispersions of the polymer P takes place according to the invention by free-radical aqueous emulsion polymerization the said monomers A, B and optionally C in Presence of at least one free-radical polymerization initiator and optionally a surfactant.
  • Radical polymerization initiators are all those in consideration, which are capable of a radical aqueous To initiate emulsion polymerization. It can be both about Peroxides, e.g. Alkali metal peroxodisulfates as well as azo compounds act. As polymerization initiators are often called.
  • Redox initiators used which consists of at least one organic Reducing agent and at least one peroxide and / or hydroperoxide are composed, e.g. tert-butyl hydroperoxide with sulfur compounds, e.g.
  • Ascorbic acid / iron (II) sulfate / hydrogen peroxide wherein instead of ascorbic also often the sodium salt hydroxymethanesulfinic acid, acetone bisulfite adduct, sodium sulfite, Sodium hydrogen sulfite or sodium bisulfite and instead of hydrogen peroxide organic peroxides such as tert-butyl hydroperoxide or alkali peroxodisulfates and / or ammonium peroxodisulfate be used.
  • preferred initiators are peroxodisulfates, such as sodium peroxodisulfate.
  • the amount of radical initiator systems used based on the total amount of the monomers to be polymerized, 0.1 to 2 wt .-%.
  • Surfactant suitable for carrying out the emulsion polymerization Substances are the ones commonly used for these purposes used protective colloids and emulsifiers.
  • the surface-active Substances are usually added in amounts of up to 10% by weight, preferably 0.5 to 5 wt .-% and in particular 1.0 to 4 wt .-%, used based on the monomers to be polymerized.
  • Suitable protective colloids are, for example, polyvinyl alcohols, Starch and cellulose derivatives or vinylpyrrolidone containing Copolymers.
  • a detailed description of further suitable Protective colloids can be found in Houben-Weyl, Methods of Organic Chemie, Volume XIV / 1, Macromolecular substances, Georg-Thieme-Verlag, Stuttgart 1961, p. 411-420.
  • the surface-active substances used are preferably exclusively emulsifiers whose relative molecular weights, in contrast to the protective colloids, are usually below 2000. They can be both anionic and nonionic in nature.
  • the anionic emulsifiers include alkali metal and ammonium salts of alkyl sulfates (alkyl radical: C 8 -C 12 ), of sulfuric monoesters of ethoxylated alkanols (EO degree: 2 to 50, alkyl radical: C 12 to C 18 ) and ethoxylated alkylphenols (EO degree: 3 to 50, alkyl radical: C 4 -C 9 ), of alkylsulfonic acids (alkyl radical: C 12 -C 18 ) and of alkylarylsulfonic acids (alkyl radical: C 9 to C 18 ), furthermore compounds of general formula I, wherein R 1 and R 2 are hydrogen or C 4 -C 24 -alkyl, preferably C 8 -C 16 -
  • Suitable nonionic emulsifiers are araliphatic or aliphatic nonionic emulsifiers, for example ethoxylated mono-, di- and trialkylphenols (EO degree: 3 to 50, alkyl radical: C 4 -C 9 ), ethoxylates of long-chain alcohols (EO degree: 3 to 50, alkyl radical : C 8 -C 36 ), as well as polyethylene oxide / polypropylene oxide block copolymers.
  • ethoxylates of long-chain alkanols alkyl radical: C 10 -C 22 , average degree of ethoxylation: 3 to 50
  • ethoxylates of long-chain alkanols alkyl radical: C 10 -C 22 , average degree of ethoxylation: 3 to 50
  • anionic emulsifiers In particular, combinations of at least one anionic and one nonionic emulsifier or combinations of two anionic emulsifiers are preferred.
  • emulsifiers can be found in Houben-Weyl, Methoden of organic chemistry, Volume XIV / 1, Macromolecular substances, Georg Thieme Verlag, Stuttgart, 1961, pp. 192-208.
  • the molecular weight of the polymers P can be reduced by adding Quantities, usually up to 2 wt .-%, based on the polymerized Monomers, one or more, the molecular weight regulatory substances, e.g. organic thio compounds, silanes, Allyl alcohols or aldehydes can be adjusted.
  • Quantities usually up to 2 wt .-%, based on the polymerized Monomers, one or more, the molecular weight regulatory substances, e.g. organic thio compounds, silanes, Allyl alcohols or aldehydes can be adjusted.
  • the emulsion polymerization can be both continuous and according to the batch procedure, preferably after a semi-continuous Procedure done.
  • the bulk i. at least 70%, preferably at least 90% of the monomers to be polymerized continuously, including stepwise or gradient mode, the polymerization batch fed.
  • This procedure is also called monomer feed designated.
  • monomer feed is meant liquid monomer mixtures, monomer solutions or in particular aqueous monomer emulsions.
  • seed-free production method can be used to set a defined polymer particle size after the emulsion polymerization the seed latex process or in the presence of in situ produced Seed latex.
  • Methods for this are known and can be taken from the prior art (see EP-B 40419, EP-A-614 922, EP-A-567 812 and literature cited therein as well as Encyclopedia of Polymer Science and Technology, Vol. 5, John Wiley & Sons Inc., New York 1966, p. 847).
  • the seed latex can also be prepared in situ from those to be polymerized Monomers are produced by first a small Amount of monomers to be polymerized as an aqueous emulsion together with a part of the surfactant, this emulsion is heated to polymerization and then a Part of the initiator in one serving.
  • Polymerization pressure and polymerization temperature are of secondary importance Importance. In general, one works at temperatures between room temperature and 120 ° C, preferably at temperatures from 40 to 95 ° C and more preferably between 50 and 90 ° C.
  • the novel aqueous polymer dispersions largely free of odorants, such as Residual monomers and other organic volatiles shape.
  • This can be done physically in a manner known per se by distillative removal (in particular via steam distillation) or by stripping with an inert gas become.
  • the lowering of the residual monomers can continue chemically by free radical postpolymerization, in particular under the action of redox initiator systems, e.g. in the DE-A 44 35 423 are listed, carried out.
  • the dispersions of the polymer P are before their Use in the preparations according to the invention, preferably by duch Addition of a nonvolatile base, e.g. Alkali metal or alkaline earth metal hydroxides or nonvolatile amines, to a pH adjusted in the range of pH 6 to pH 10.
  • a nonvolatile base e.g. Alkali metal or alkaline earth metal hydroxides or nonvolatile amines
  • dispersions In the way of emulsion polymerization are basically dispersions with solids contents up to about 80% by weight (polymer content, based on the total weight of the dispersion). For practical reasons are usually for the inventive Preparations Polymerisate dispersions with solids contents in the range of 40 to 70 wt .-% preferred. Especially preferred become dispersions with polymer contents of about 50 Wt .-%. Of course, dispersions are also lower solids content in principle for the preparations according to the invention used.
  • the polymers P are in the form of their aqueous polymer dispersions as a binder in such pigment-containing Preparations used for coating substrates serve (pigment-containing coating agent).
  • pigment-containing coating agent for example, plastic dispersion plasters, tile adhesives, paints, Sealants or sealants, in particular for porous components.
  • a preferred embodiment of the present invention relates Preparations in the form of emulsion paints, in particular for outdoor applications.
  • the coatings available therefrom are characterized in particular by a very low soiling tendency and excellent weathering stability.
  • Typical pigments for the preparations according to the invention are titanium dioxide, preferably in rutile, barium sulfate, zinc oxide, zinc sulfide, basic Lead carbonate, antimony trioxide, lithopone (zinc sulfide + barium sulfate).
  • the preparations may, however, also colored pigments, for example Iron oxides, carbon black, graphite, luminescent pigments, Zinc Yellow, Zinc Green, Ultramarine, Manganese Black, Antimony Black, Manganese violet, Paris blue or Schweinfurter green included.
  • Suitable fillers include aluminosilicates, such as feldspars, silicates, such as kaolin, talc, mica, magnesite, alkaline earth carbonates, such as calcium carbonate, for example in the form of calcite or Chalk, magnesium carbonate, dolomite, alkaline earth sulphates, such as calcium sulphate, Silica etc.
  • the fillers can be used as individual components be used. In practice, filler mixtures have especially proven, e.g. Calcium carbonate / kaolin, Calcium carbonate / talc.
  • Fillers e.g. finely divided calcium carbonate or mixtures different calcium carbonates with different particle sizes used.
  • hue and the color depth are preferably blends of color pigments and fillers used.
  • auxiliaries iv) include wetting or dispersing agents, such as sodium, potassium or ammonium polyphosphates, alkali metal and ammonium salts of polyacrylic acids and polymaleic acid, Polyphosphonates such as 1-hydroxyethane-1,1-diphosphonic acid Sodium and Naphthalinsulfonklaresalze, in particular their sodium salts.
  • the dispersants are usually in one Amount of 0.1 to 0.6 wt .-% based on the total weight of Dispersion paint used.
  • the aids include iv also defoamers, preservatives or water repellents, Biocides, fibers or other ingredients.
  • auxiliaries iv) optionally also include Thickeners, for example cellulose derivatives, such as methylcellulose, Hydroxyethylcellulose and carboxymethylcellulose, further Casein, gum arabic, gum tragacanth, starch, sodium alginate, Polyvinyl alcohol, polyvinylpyrrolidone, sodium polyacrylates, water-soluble Acrylic and methacrylic acid based copolymers, such as acrylic acid / acrylamide and methacrylic acid / acrylic ester copolymers and so-called associative thickeners, for example styrene-maleic anhydride polymers or preferably hydrophobically modified Polyether urethanes, as described, for example, by N. Chen et al. in J.
  • Thickeners for example cellulose derivatives, such as methylcellulose, Hydroxyethylcellulose and carboxymethylcellulose, further Casein, gum arabic, gum tragacanth, starch, sodium alginate, Polyvinyl alcohol, polyvinylpyrroli
  • inorganic thickeners e.g. Bentonite or hectorite can be used.
  • Thickeners are generally used in amounts of 0.1 to 3 wt .-%, preferably 0.1 to 1 wt .-%, based on the total weight the aqueous preparation used.
  • the coating compositions of the invention are stable fluid systems, which is used to coat a variety of substrates can use. Suitable substrates are for example wood, concrete, Metal, Glass, Ceramics, Plastic, Plaster, Wallpaper, Painted, primed or weathered surfaces.
  • the application the coating agent is applied to the substrate to be coated in a dependent on the design of the preparation Wise.
  • the application can, depending on viscosity and pigment content and the substrate by means of rollers, brushes, squeegees or as a spray.
  • the coating compositions of the invention Can be used both as a topcoat for primed and for unprimed Substrates and used as a primer, the latter usually having a lower solids content.
  • the coating compositions of the invention are characterized by a good weathering stability and a good wet abrasion resistance out. Their soiling tendency, especially in applications in the Outdoors is compared to conventional coating agents on the Base softer binder significantly improved. An improvement also results over conventional, solvent-containing Coating agents.
  • the mean particle size (z mean) of the polymer particles was determined by dynamic light scattering (photon correlation spectroscopy) on a 0.01 wt .-% dispersion in water at 23 ° C. by means of an autosizer IIc from Malvern Instruments, England. Given is the mean diameter of the cumulant evaluation (cumulant z-average) of the measured autocorrelation function.
  • the dispersions D2 and D4 were blended with the following ingredients in the order given. First, successively with stirring 89 g deionized water 2 g dispersants 3 g preservative 4 g aqueous sodium polyphosphate solution (25% strength by weight) 60 g aqueous thickener solution A (2% strength by weight) 2 g defoamers 2 g caustic soda (20% strength by weight) 157 g Titanium dioxide 182 g calcium carbonate 56 g Talcum (5 ⁇ m) combined and mixed for 20 minutes. This was added with stirring 1 g defoamers 382 g aqueous polymer dispersion (about 50% strength by weight) 50 g aqueous thickener solution B (5% strength by weight) and 10 g water
  • a solvent-based paint VB1 formulated. This contained the for B1 specified ingredients in the amounts specified therein.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Structural Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Claims (9)

  1. Revêtements aqueux pigmentés, présentant une concentration volumique en pigment CVP de l'ordre de 25 à 55 et essentiellement exempts de composés organiques volatils, contenant :
    (i) au moins une dispersion aqueuse de polymère, filmogène à la température ambiante, d'au moins un polymère P, constitué de :
    80 à 99,95% en poids d'au moins un monomère A, choisi parmi les esters de l'acide acrylique avec des alcanols en C2 à C20 ou des cycloalcanols en C5 à C10, et les esters de l'acide méthacrylique avec des alcanols en C1 à C20 ou des cycloalcanols en C5 à C10,
    0,05 à 10% en poids d'au moins un monomère B, choisi parmi des acides carboxyliques à insaturation éthylénique, des acides sulfoniques à insaturation éthylénique ou des acides phosphoniques à insaturation éthylénique et leurs sels, ainsi que
    0 à 20% en poids d'un ou plusieurs monomères C, différents des monomères A et B,
    (ii) au moins un pigment inorganique et le cas échéant des matières de remplissage inorganiques ou organiques,
    (iii) 0,05 à moins de 0,3% en poids, par rapport au polymère P, d'au moins un photoinitiateur non polymérisable,
    (iv) de l'eau et des adjuvants usuels.
  2. Revêtements selon la revendication 1, contenant moins de 0,1% en poids de composés organiques volatils.
  3. Revêtements selon la revendication 1 ou 2, dans lesquels le photoinitiateur est choisi parmi la benzophénone et ses dérivés.
  4. Revêtements selon l'une quelconque des revendications qui précèdent, dans lesquels la dispersion aqueuse du polymère P présente une température minimale de formation de film TMF de moins de 10°C.
  5. Revêtements selon l'une quelconque des revendications qui précèdent, dans lesquels les monomères A comprennent, par rapport au poids total des monomères A,
    de 25 à 55% en poids d'au moins un ester de l'acide méthacrylique avec un alcanol en C1 à C4 et
    de 45 à 75% en poids d'au moins un ester de l'acide acrylique avec un alcanol en C2 à C10.
  6. Revêtements selon l'une quelconque des revendications qui précèdent, dans lesquels les monomères C sont choisis parmi les amides d'acides carboxyliques à insaturation monoéthylénique.
  7. Revêtements dans lesquels la proportion pondérale du polymère P à la quantité totale de pigment et de matières de remplissage est de l'ordre de 2 : 1 à 1 : 8.
  8. Revêtements selon l'une quelconque des revendications qui précèdent, sous la forme d'une peinture à dispersion pour applications extérieures.
  9. Procédé de revêtement de substrats, caractérisé en ce que l'on applique un revêtement selon l'une quelconque des revendications 1 à 8 sur le substrat à revêtir.
EP00108646A 1999-04-21 2000-04-20 Revêtements aqueux pigmentés Expired - Lifetime EP1046682B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19918052A DE19918052A1 (de) 1999-04-21 1999-04-21 Wässrige, pigmenthaltige Beschichtungsmittel
DE19918052 1999-04-21

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EP1046682B1 true EP1046682B1 (fr) 2005-11-16

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EP (1) EP1046682B1 (fr)
JP (1) JP2000327988A (fr)
DE (2) DE19918052A1 (fr)
ES (1) ES2253154T3 (fr)

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JP2000327988A (ja) 2000-11-28
DE19918052A1 (de) 2000-10-26
US6376570B1 (en) 2002-04-23
ES2253154T3 (es) 2006-06-01
EP1046682A1 (fr) 2000-10-25
DE50011602D1 (de) 2005-12-22

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